注意缺陷/多动障碍患者的临床和安全性评价

T. Allen, Rashash Dhoalokia, Sylvia Johnson-Park, Giridhar Mnv, Naveed Basha Court
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摘要

背景:注意缺陷/多动障碍(ADHD)是儿童最常见的神经发育障碍之一。它通常在儿童时期首次被诊断出来,通常持续到成年。患有多动症的儿童很难集中注意力、控制冲动行为或过于活跃。其特征是多动、冲动和注意力不集中,超出了儿童年龄的合理发展预期。Brillia背后的科学是基于一种结合顺势疗法和抗体科学的新方法。宝莲的有效成分,Lapine S-100免疫球蛋白,是使用大脑特异性S-100蛋白(S-100B)的抗体产生的。该蛋白是许多不同的细胞内和细胞外脑过程的重要调节因子,例如各种酶活性,钙稳态,神经元之间的通信等。因此,对小儿布里安治疗焦虑症、行为障碍、注意力障碍、伴兴奋性增加、易怒和多动的临床研究是非常重要和有希望的。为了确定brilliant for Children治疗儿童焦虑症、行为障碍和注意力障碍,并伴有易兴奋、易怒和多动症的疗效,进行了两项临床研究。方法:采用双盲、随机、安慰剂对照研究,评价Brillia治疗儿童注意缺陷多动障碍的临床疗效和安全性。在纳入研究之前,向患者或其法定监护人提供了有关研究的信息,并签署了知情同意书。在研究期间收集的患者信息是严格保密的。*通讯:Timothy Allen, Global Allied Pharmaceuticals,卓越研发中心,160 Vista Oak Dr. Longwood, FL 32779, USA, E-mail: timallenmed69@gmail.com
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and safety evaluation of Brillia patients with Attention-Deficit/Hyperactivity Disorder
Background: Attention-Deficit/Hyperactivity Disorder (ADHD) is one of the most common neurodevelopmental disorders in children. It is usually first diagnosed in childhood and often lasts into adulthood. Children with ADHD will have trouble paying attention, controlling impulsive behaviors, or be overly active. The hallmarks are hyperactivity, impulsivity, and inattention that are beyond reasonable developmental expectations for a child's age. The science behind Brillia is based on a new way to combine homeopathy and antibody science. The active ingredient of Brillia, Lapine S-100 immune globulin, is produced using antibodies to the brainspecific S-100 protein (S-100B). This protein is an essential regulator of many different intracellular and extracellular brain processes, e.g., various enzyme activities, calcium homeostasis, communication between neurons, etc. Thus, the clinical study of the efficacy of Brillia for Children for the treatment of anxiety disorders, disturbances of behavior, and attention, accompanied by increased excitability, irritability, and hyperactivity, are very important and promising. To determine the efficacy of Brillia for Children for the treatment of anxiety disorders, disturbances of behavior, and attention, accompanied by increased excitability, irritability, and hyperactivity in children, two clinical studies were carried out. Methods: A double-blind, randomized placebo-controlled study of Brillia evaluating clinical efficacy and safety for children with attention deficit hyperactivity disorder was conducted. Prior to inclusion in the study, the patients or their legal guardians were provided with information about the study and signed an informed consent form. Patient information collected during the study is strictly confidential. *Correspondence to: Timothy Allen, Global Allied Pharmaceuticals, Center for Excellence in Research and Development, 160 Vista Oak Dr. Longwood, FL 32779, USA, E-mail: timallenmed69@gmail.com
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